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Thromboelastography to Study Burn Coagulopathy

The Use of Thromboelastography in Burn Injury to Improve Burn Coagulopathy Evaluation and Intervention

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06879509
Enrollment
50
Registered
2025-03-17
Start date
2025-06-30
Completion date
2025-08-31
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn, Coagulation, Blood

Keywords

burn, coagulation, Thromboelastography

Brief summary

This pilot study examines the use of thromboelastography (TEG), a specialized blood test, to evaluate clotting abnormalities in burn patients. The study aims to understand how burn injuries impact the body's ability to form and break down blood clots over time. Specifically, the investigators will research whether the percentage of total body surface area burned (%TBSA) is associated with changes in blood clotting, track the evolution of clotting patterns during the first four weeks following a burn injury, and explore whether these changes can predict recovery or complications. By providing new insights into clotting dynamics in burn patients, the study seeks to improve diagnostic methods, enhance monitoring strategies, and guide treatments to optimize patient care and outcomes.

Interventions

DIAGNOSTIC_TESTThromboelastography

All participants will receive this intervention. Thromboelastography (TEG) is a blood test that provides a detailed assessment of the clotting process, measuring how blood clots form, strengthen, and dissolve. It offers real-time insights into a patient's coagulation status, helping to identify clotting disorders and guide treatment decisions.

Sponsors

Francesco Egro
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients admitted with acute burn injuries * Aged 18 years and older * Provided consent to participate in the study

Exclusion criteria

* Patients with a history of venous thromboembolism or hyper/hypocoagulopathy

Design outcomes

Primary

MeasureTime frameDescription
ThromboelastographyDuration of hospital length of stay, up to 28 daysThromboelastography (TEG) evaluates blood's clotting ability by measuring the strength and elasticity of a clot over time, producing a dynamic graph. The following outcome measures will be assessed at specific time points (Day 1, Day 7, Day 14, Day 21, and Day 28): 1. Reaction Time (R) (seconds) - The time from test initiation until the first detectable clot formation. 2. Kinetic Time (K) (seconds) - The time from initial clot formation to a defined clot strength threshold. 3. Maximum Amplitude (MA) (millimeters) - The peak strength of the formed clot. 4. Alpha Angle (degrees) - The slope of the clot formation curve, representing the rate of clot development. 5. Lysis at 30 Minutes (Ly30) (percentage of MA) - The percentage of clot degradation occurring 30 minutes after reaching maximum amplitude. Each parameter will be measured at the specified time points, and values will be aggregated into one TEG graph.

Secondary

MeasureTime frameDescription
Hospital Length of StayDuration of hospital length of stay, up to 28 daysThe investigators will measure the number of days patients stay in the hospital for treatment.
Complications During TreatmentDuration of hospital length of stay, up to 28 daysThe investigators will record any complications, such as infections, graft loss, flap loss, or thrombosis that occur during treatment.

Countries

United States

Contacts

Primary ContactFrancesco M Egro, MD
egrofm@upmc.edu(404) 861-7944‬
Backup ContactHilary Y Liu, BS
liuh23@upmc.edu4846315188

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026